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Thiophene-2-sulfonamide

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CAS:6339-87-3
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Thiophene-2-sulfonamide manufacturers

  • 2-Thiophenesulfonamide
  • 2-Thiophenesulfonamide pictures
  • $1.00 / 1KG
  • 2020-02-04
  • CAS:6339-87-3
  • Min. Order: 1KG
  • Purity: Min98% HPLC
  • Supply Ability: g/kg/ton
Thiophene-2-sulfonamide Basic information
Product Name:Thiophene-2-sulfonamide
Synonyms:BUTTPARK 44\07-11;2-Thienylsulfonamide;2-Thiophenesulfonamide(6CI,7CI,8CI,9CI);THIOPHENE-2-SULFONIC ACID AMIDE;Thiophene-2-sulphonamide;THIOPHENE-2-SULFONAMIDE;THIOPHENE-ALPHA-SULFONAMIDE;THIOPHENE-A-SULFONAMIDE
CAS:6339-87-3
MF:C4H5NO2S2
MW:163.22
EINECS:
Product Categories:Heterocycle-oher series;Thiophene intermediates;Building Blocks;C4 to C6;Chemical Synthesis;Heterocyclic Building Blocks;Thiophenes;SULFONAMIDE
Mol File:6339-87-3.mol
Thiophene-2-sulfonamide Structure
Thiophene-2-sulfonamide Chemical Properties
Melting point 137-141 °C
Boiling point 338.1±34.0 °C(Predicted)
density 1.513±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility soluble in Methanol
form powder to crystal
pka9.94±0.60(Predicted)
color White to Light yellow to Light orange
InChI1S/C4H5NO2S2/c5-9(6,7)4-2-1-3-8-4/h1-3H,(H2,5,6,7)
InChIKeyKTFDYVNEGTXQCV-UHFFFAOYSA-N
SMILESNS(=O)(=O)c1cccs1
CAS DataBase Reference6339-87-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26
WGK Germany 3
RTECS XN0294000
HS Code 29350090
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
Thiophene-2-sulfonamide Usage And Synthesis
DefinitionChEBI: 2-Thiophenesulfonamide is a member of thiophenes.
Synthesis Reference(s)Tetrahedron Letters, 35, p. 7201, 1994 DOI: 10.1016/0040-4039(94)85360-6
Synthesis
2-Thiophenesulfonyl chloride

16629-19-9

Thiophene-2-sulfonamide

6339-87-3

General procedure for the synthesis of 2-thiophenesulfonamide from 2-thiophenesulfonyl chloride: Example: preparation of 2-thiophenesulfonamide 2-Thiophenesulfonyl chloride (0.5 g, 2.74 mmol) was added to 25% ammonium hydroxide solution (5 mL, 33.45 mmol), refluxed and stirred at 50°C for 15 hours. Upon completion of the reaction, the reaction mixture was filtered while hot and the residue was washed with boiling aqueous 25% ammonium hydroxide solution. Subsequently, the ammonium hydroxide solution was removed by vacuum distillation until there was no ammonia odor. Eventually, 2-thiophenesulfonamide was recrystallized from water to give a white solid (0.328 g, 77% yield). Product Characterization: Melting point: 145-146°C; IR spectrum (KBr, cm?1): 3290 (N-H stretching vibration), 3224 (N-H stretching vibration); NMR hydrogen spectrum (400 MHz, DMSO-d6, δ): 7.15 (1H, dd, J = 5.0, 3.7 Hz, C(4)H), 7.55 (1H, dd, J = 3.7, 1.4 Hz, C(3)H), 7.66 (2H, s, NH2), 7.85 (1H, dd, J = 5.0, 1.4 Hz, C(5)H); NMR carbon spectrum (100 MHz, DMSO-d6, δ): 127.3, 130.0, 131.1, 145.7; Mass spectrum (ESI?): m/z 162 ([M-H]? , 100%); High-resolution mass spectrum (ESI?): C4H4NO2S2 ([M-H]?) Calculated value 161.9689, measured value 161.9695.

References[1] Journal of the American Chemical Society, 2010, vol. 132, # 10, p. 3238 - 3239
[2] Patent: WO2011/55142, 2011, A2. Location in patent: Page/Page column 47
[3] Phosphorus and Sulfur and the Related Elements, 1981, vol. 10, p. 111 - 120
[4] Phosphorus and Sulfur and the Related Elements, 1980, vol. 8, p. 197 - 200
[5] Justus Liebigs Annalen der Chemie, 1933, vol. 501, p. 174,182
Thiophene-2-sulfonamide Preparation Products And Raw materials
Raw materials2-Thiophenesulfonyl chloride-->Ammonium hydroxide
Tag:Thiophene-2-sulfonamide(6339-87-3) Related Product Information
Sulfanilamide 3-Aminobenzenesulfonamide p-Toluenesulfonamide Cyclopropanesulfonamide Methanesulfonamide Thiophene Benzenesulfonamide 2-Thiazolecarboxamidine Hydrochloride 2-Thiophenecarboxylic acid 2-Thiophenecarboxaldehyde 2-Thiopheneacetyl chloride 2-Thiophenesulfonyl chloride 2-Thiopheneacetic acid 2,3-THIOPHENEDICARBOXALDEHYDE Thiophene-2-boronic acid pinacol ester Thifensulfuron methyl 2,5-Thiophenedicarboxylic acid Thieno[3,2-b]thiophene

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